389 research outputs found
Immunogold Labeling to Enhance Contrast in Optical Coherence Microscopy of Tissue Engineered Corneal Constructs
Our lab has used an optical coherence microscope (OCM) to assess both the structure of tissue-engineered corneal constructs and their transparency. Currently, we are not able to resolve cells versus collagen matrix material in the images produced. We would like to distinguish cells in order to determine if they are viable while growing in culture and also if they are significantly contributing to the light scattering in the tissue. In order to do this, we are currently investigating the use of immunogold labeling. Gold nanoparticles are high scatterers and can create contrast in images. We have conjugated gold nanoparticles to antibodies specific to the α5 ÎČ1 integrins expressed in some corneal cells. This choice of target should allow assessment of the phenotypic behavior of the cells in the tissue, as different integrins are expressed in different phenotypes. This study applies the immunogold technique to study cultured corneal cells using the OCM with the ultimate goal of monitoring cellular behavior in engineered tissue and corroborating results from standard histological methods
Superconductivity Induced by Bond Breaking in the Triangular Lattice of IrTe2
IrTe2, a layered compound with a triangular iridium lattice, exhibits a
structural phase transition at approximately 250 K. This transition is
characterized by the formation of Ir-Ir bonds along the b-axis. We found that
the breaking of Ir-Ir bonds that occurs in Ir1-xPtxTe2 results in the
appearance of a structural critical point in the T = 0 limit at xc = 0.035.
Although both IrTe2 and PtTe2 are paramagnetic metals, superconductivity at Tc
= 3.1 K is induced by the bond breaking in a narrow range of x > xc in
Ir1-xPtxTe2. This result indicates that structural fluctuations can be involved
in the emergence of superconductivity.Comment: 10 pages, 4 figure
Composability in quantum cryptography
In this article, we review several aspects of composability in the context of
quantum cryptography. The first part is devoted to key distribution. We discuss
the security criteria that a quantum key distribution protocol must fulfill to
allow its safe use within a larger security application (e.g., for secure
message transmission). To illustrate the practical use of composability, we
show how to generate a continuous key stream by sequentially composing rounds
of a quantum key distribution protocol. In a second part, we take a more
general point of view, which is necessary for the study of cryptographic
situations involving, for example, mutually distrustful parties. We explain the
universal composability framework and state the composition theorem which
guarantees that secure protocols can securely be composed to larger
applicationsComment: 18 pages, 2 figure
Cooperation, Norms, and Revolutions: A Unified Game-Theoretical Approach
Cooperation is of utmost importance to society as a whole, but is often
challenged by individual self-interests. While game theory has studied this
problem extensively, there is little work on interactions within and across
groups with different preferences or beliefs. Yet, people from different social
or cultural backgrounds often meet and interact. This can yield conflict, since
behavior that is considered cooperative by one population might be perceived as
non-cooperative from the viewpoint of another.
To understand the dynamics and outcome of the competitive interactions within
and between groups, we study game-dynamical replicator equations for multiple
populations with incompatible interests and different power (be this due to
different population sizes, material resources, social capital, or other
factors). These equations allow us to address various important questions: For
example, can cooperation in the prisoner's dilemma be promoted, when two
interacting groups have different preferences? Under what conditions can costly
punishment, or other mechanisms, foster the evolution of norms? When does
cooperation fail, leading to antagonistic behavior, conflict, or even
revolutions? And what incentives are needed to reach peaceful agreements
between groups with conflicting interests?
Our detailed quantitative analysis reveals a large variety of interesting
results, which are relevant for society, law and economics, and have
implications for the evolution of language and culture as well
A Cellular Potts Model simulating cell migration on and in matrix environments
Cell migration on and through extracellular matrix plays a critical role in a wide variety of physiological and pathological phenomena, and in scaffold-based tissue engineering. Migration is regulated by a number of extracellular matrix- or cell-derived biophysical parameters, such as matrix fiber orientation, gap size, and elasticity, or cell deformation, proteolysis, and adhesion. We here present an extended Cellular Potts Model (CPM) able to qualitatively and quantitatively describe cell migratory phenotype on both two-dimensional substrates and within three-dimensional environments, in a close comparison with experimental evidence. As distinct features of our approach, the cells are represented by compartmentalized discrete objects, differentiated in the nucleus and in the cytosolic region, while the extracellular matrix is composed of a fibrous mesh and of a homogeneous fluid. Our model provides a strong correlation of the directionality of migration with the topological ECM distribution and, further, a biphasic dependence of migration on the matrix density, and in part adhesion, in both two-dimensional and three-dimensional settings. Moreover, we demonstrate that the directional component of cell movement is strongly correlated with the topological distribution of the ECM fibrous network. In the three-dimensional networks, we also investigate the effects of the matrix mechanical microstructure, observing that, at a given distribution of fibers, cell motility has a subtle bimodal relation with the elasticity of the scaffold. Finally, cell locomotion requires deformation of the cell's nucleus and/or cell-derived proteolysis of steric fibrillar obstacles within rather rigid matrices characterized by small pores, not, however, for sufficiently large pores. In conclusion, we here propose a mathematical modeling approach that serves to characterize cell migration as a biological phenomen in health, disease and tissue engineering applications. The research that led to the present paper was partially supported by a grant of the group GNFM of INdA
The density of gold-silver-copper alloys and its calculation from the chemical composition
Predictors and outcomes in primary depression care (POKAL) â a research training group develops an innovative approach to collaborative care
BACKGROUND: The interdisciplinary research training group (POKAL) aims to improve care for patients with depression and multimorbidity in primary care. POKAL includes nine projects within the framework of the Chronic Care Model (CCM). In addition, POKAL will train young (mental) health professionals in research competences within primary care settings. POKAL will address specific challenges in diagnosis (reliability of diagnosis, ignoring suicidal risks), in treatment (insufficient patient involvement, highly fragmented care and inappropriate long-time anti-depressive medication) and in implementation of innovations (insufficient guideline adherence, use of irrelevant patient outcomes, ignoring relevant context factors) in primary depression care. METHODS: In 2021 POKAL started with a first group of 16 trainees in general practice (GPs), pharmacy, psychology, public health, informatics, etc. The program is scheduled for at least 6Â years, so a second group of trainees starting in 2024 will also have three years of research-time. Experienced principal investigators (PIs) supervise all trainees in their specific projects. All projects refer to the CCM and focus on the diagnostic, therapeutic, and implementation challenges. RESULTS: The first cohort of the POKAL research training group will develop and test new depression-specific diagnostics (hermeneutical strategies, predicting models, screening for suicidal ideation), treatment (primary-care based psycho-education, modulating factors in depression monitoring, strategies of de-prescribing) and implementation in primary care (guideline implementation, use of patient-assessed data, identification of relevant context factors). Based on those results the second cohort of trainees and their PIs will run two major trials to proof innovations in primary care-based a) diagnostics and b) treatment for depression. CONCLUSION: The research and training programme POKAL aims to provide appropriate approaches for depression diagnosis and treatment in primary care
In vitro studies and preliminary in vivo evaluation of silicified concentrated collagen hydrogels
Hybrid and nanocomposite silicacollagen materials derived from concentrated collagen hydrogels were evaluated in vitro and in vivo to establish their potentialities for biological dressings. Silicification significantly improved the mechanical and thermal stability of the collagen network within the hybrid systems. Nanocomposites were found to favor the metabolic activity of immobilized human dermal fibroblastswhile decreasing the hydrogel contraction. Cell adhesion experiments suggested that in vitro cell behavior was dictated by mechanical properties and surface structure of the scaffold. First-to-date in vivo implantation of bulk hydrogels in subcutaneous sites of rats was performed over the vascular inflammatory period. These materials were colonized and vascularized without inducing strong inflammatory response. These data raise reasonable hope for the future application of silicacollagen biomaterials as biological dressings.Fil: Desimone, MartĂn Federico. Consejo Nacional de Investigaciones CientĂficas y TĂ©cnicas. Oficina de CoordinaciĂłn Administrativa Houssay. Instituto de QuĂmica y Metabolismo del FĂĄrmaco. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂmica. Instituto de QuĂmica y Metabolismo del FĂĄrmaco; ArgentinaFil: HĂ©lary, Christophe. UniversitĂ© Pierre et Marie Curie; FranciaFil: Quignard, Sandrine. UniversitĂ© Pierre et Marie Curie; FranciaFil: Rietveld, Ivo B. Universite de Paris; FranciaFil: Bataille, Clement. UniversitĂ© de Versailles Saint-quentin-en-yvelines.; FranciaFil: Copello, Guillermo Javier. Consejo Nacional de Investigaciones CientĂficas y TĂ©cnicas. Oficina de CoordinaciĂłn Administrativa Houssay. Instituto de QuĂmica y Metabolismo del FĂĄrmaco. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂmica. Instituto de QuĂmica y Metabolismo del FĂĄrmaco; ArgentinaFil: Mosser, Gervaise. UniversitĂ© Pierre et Marie Curie; FranciaFil: Giraud Guille, Marie-Madeleine. UniversitĂ© Pierre et Marie Curie; FranciaFil: Livage, Jacques. UniversitĂ© Pierre et Marie Curie; FranciaFil: Meddahi PellĂ©, Anne. UniversitĂ© de Versailles Saint-quentin-en-yvelines.; FranciaFil: Coradin, Thibaud. UniversitĂ© Pierre et Marie Curie; Franci
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